Circular RNA—Is the Circle Perfect?
Caba, Lavinia, Florea, Laura, Gug, Cristina, Dimitriu, Daniela Cristina, Gorduza, Eusebiu Vlad
Published in Biomolecules (24.11.2021)
Published in Biomolecules (24.11.2021)
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Journal Article
Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance
Florea, Laura, Caba, Lavinia, Gorduza, Eusebiu Vlad
Published in Frontiers in Pediatrics (03.06.2022)
Published in Frontiers in Pediatrics (03.06.2022)
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Journal Article
A Scoping Review of the Relationship between Intermittent Fasting and the Human Gut Microbiota: Current Knowledge and Future Directions
Popa, Alina Delia, Niță, Otilia, Gherasim, Andreea, Enache, Armand Iustinian, Caba, Lavinia, Mihalache, Laura, Arhire, Lidia Iuliana
Published in Nutrients (26.04.2023)
Published in Nutrients (26.04.2023)
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Journal Article
Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare Disorder
Balinisteanu, Ioana, Caba, Lavinia, Florea, Andreea, Popescu, Roxana, Florea, Laura, Ungureanu, Maria-Christina, Leustean, Letitia, Gorduza, Eusebiu Vlad, Preda, Cristina
Published in Current Issues in Molecular Biology (01.08.2024)
Published in Current Issues in Molecular Biology (01.08.2024)
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Journal Article
Genomics and Epigenomics in the Molecular Biology of Melanoma—A Prerequisite for Biomarkers Studies
Zob, Daniela Luminita, Augustin, Iolanda, Caba, Lavinia, Panzaru, Monica-Cristina, Popa, Setalia, Popa, Alina Delia, Florea, Laura, Gorduza, Eusebiu Vlad
Published in International journal of molecular sciences (31.12.2022)
Published in International journal of molecular sciences (31.12.2022)
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Journal Article
Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome
Ciobanu, Cristian-Gabriel, Nucă, Irina, Popescu, Roxana, Antoci, Lucian-Mihai, Caba, Lavinia, Ivanov, Anca Viorica, Cojocaru, Karina-Alexandra, Rusu, Cristina, Mihai, Cosmin-Teodor, Pânzaru, Monica-Cristina
Published in International journal of molecular sciences (24.05.2023)
Published in International journal of molecular sciences (24.05.2023)
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Journal Article
Gorham-Stout Disease with Multiple Bone Involvement—Challenging Diagnosis of a Rare Disease and Literature Review
Momanu, Alina, Caba, Lavinia, Gorduza, Nicoleta Carmen, Arhire, Oana Elena, Popa, Alina Delia, Ianole, Victor, Gorduza, Eusebiu Vlad
Published in Medicina (02.07.2021)
Published in Medicina (02.07.2021)
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Journal Article
Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity
Pânzaru, Monica-Cristina, Caba, Lavinia, Florea, Laura, Braha, Elena Emanuela, Gorduza, Eusebiu Vlad
Published in Diagnostics (27.05.2022)
Published in Diagnostics (27.05.2022)
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Journal Article
From the Sun to the Cell: Examining Obesity through the Lens of Vitamin D and Inflammation
Popa, Alina Delia, Niță, Otilia, Caba, Lavinia, Gherasim, Andreea, Graur, Mariana, Mihalache, Laura, Arhire, Lidia Iuliana
Published in Metabolites (20.12.2023)
Published in Metabolites (20.12.2023)
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Journal Article
Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population
Gug, Cristina, Mozos, Ioana, Ratiu, Adrian, Tudor, Anca, Gorduza, Eusebiu Vlad, Caba, Lavinia, Gug, Miruna, Cojocariu, Catalina, Furau, Cristian, Furau, Gheorghe, Vaida, Monica Adriana, Stoicanescu, Dorina
Published in Medicina (05.01.2022)
Published in Medicina (05.01.2022)
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Journal Article
Hydatidiform Mole-Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative Review
Florea, Andreea, Caba, Lavinia, Grigore, Ana-Maria, Antoci, Lucian-Mihai, Grigore, Mihaela, Gramescu, Mihaela I, Gorduza, Eusebiu Vlad
Published in Life (10.12.2023)
Published in Life (10.12.2023)
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Journal Article
Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street
Balinisteanu, Ioana, Panzaru, Monica-Cristina, Caba, Lavinia, Ungureanu, Maria-Christina, Florea, Andreea, Grigore, Ana Maria, Gorduza, Eusebiu Vlad
Published in Biomedicines (29.07.2023)
Published in Biomedicines (29.07.2023)
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Journal Article
Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review
Resmerita, Irina, Cozma, Romica Sebastian, Popescu, Roxana, Radulescu, Luminita Mihaela, Panzaru, Monica Cristina, Butnariu, Lacramioara Ionela, Caba, Lavinia, Ilie, Ovidiu-Dumitru, Gavril, Eva-Cristiana, Gorduza, Eusebiu Vlad, Rusu, Cristina
Published in Genes (15.12.2020)
Published in Genes (15.12.2020)
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Journal Article
Observational study on dietary patterns in pregnancy
POPA, Alina Delia, CABA, Lavinia, ENACHE, Armand, MIHALACHE, Carmen, ANTOHE, Ileana
Published in Practica medicală (2006) (30.06.2021)
Published in Practica medicală (2006) (30.06.2021)
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Journal Article
A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature
Popescu, Roxana, Grămescu, Mihaela, Caba, Lavinia, Pânzaru, Monica-Cristina, Butnariu, Lăcrămioara, Braha, Elena, Popa, Setalia, Rusu, Cristina, Cardos, Georgeta, Zeleniuc, Monica, Martiniuc, Violeta, Gug, Cristina, Păduraru, Luminiţa, Stamatin, Maria, Diaconu, Carmen C, Gorduza, Eusebiu Vlad
Published in Genes (07.12.2021)
Published in Genes (07.12.2021)
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Journal Article
Clinical Aspects of a Rare Disease: Bardet Biedl Syndrome
FOCSA, Ina Ofelia, BUDISTEANU, Magdalena, STOICA, Cristina, NEDELEA, Florina, JURCA, Claudia, CABA, Lavinia, PANZARU, Monica, RUSU, Cristina, BALGRADEAN, Mihaela, BUTNARIU, Lacramioara
Published in Medicina modernă (Bucharest, Romania) (30.03.2022)
Published in Medicina modernă (Bucharest, Romania) (30.03.2022)
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Journal Article
Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome
Antohi, Cristina, Haba, Danisia, Caba, Lavinia, Ciofu, Mihai Liviu, Drug, Vasile-Liviu, Bărboi, Oana-Bogdana, Dobrovăț, Bogdan Ionuț, Pânzaru, Monica-Cristina, Gorduza, Nicoleta Carmen, Lupu, Vasile Valeriu, Dimofte, Doina, Gug, Cristina, Gorduza, Eusebiu Vlad
Published in Diagnostics (01.09.2021)
Published in Diagnostics (01.09.2021)
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Journal Article
Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and review of the literature
Gug, Cristina, Caba, Lavinia, Mozos, Ioana, Stoian, Dana, Atasie, Diter, Gug, Miruna, Gorduza, Eusebiu Vlad
Published in Gene (30.05.2020)
Published in Gene (30.05.2020)
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